The lincRNA MIRAT binds to IQGAP1 and modulates the MAPK pathway in NRAS mutant melanoma.
Martina SanlorenzoIgor VujicRosaura Esteve-PuigKevin LaiMarin VujicKevin LinChristian PoschMichelle DimonAdrian MoyMitchell ZekhtserKatia JohnstonDeborah GhoWilson HoAbhinay GajjalaJuan A Oses-PrietoAlma BurlingameAdil I DaudKlemens RappersbergerSusana Ortiz-UrdaPublished in: Scientific reports (2018)
Despite major advances in targeted melanoma therapies, drug resistance limits their efficacy. Long noncoding RNAs (lncRNAs) are transcriptome elements that do not encode proteins but are important regulatory molecules. LncRNAs have been implicated in cancer development and response to different therapeutics and are thus potential treatment targets; however, the majority of their functions and molecular interactions remain unexplored. In this study, we identify a novel cytoplasmic intergenic lincRNA (MIRAT), which is upregulated following prolonged MAPK inhibition in NRAS mutant melanoma and modulates MAPK signaling by binding to the MEK scaffold protein IQGAP1. Collectively, our results present MIRAT's direct modulatory effect on the MAPK pathway and highlight the relevance of cytoplasmic lncRNAs as potential targets in drug resistant cancer.
Keyphrases
- drug resistant
- signaling pathway
- pi k akt
- papillary thyroid
- wild type
- oxidative stress
- multidrug resistant
- squamous cell
- acinetobacter baumannii
- network analysis
- skin cancer
- small molecule
- single cell
- lymph node metastasis
- rna seq
- transcription factor
- childhood cancer
- basal cell carcinoma
- cell proliferation
- risk assessment
- young adults
- genome wide analysis
- climate change